US4725665A - Use of salts of water-soluble - Google Patents
Use of salts of water-soluble Download PDFInfo
- Publication number
- US4725665A US4725665A US06/888,351 US88835186A US4725665A US 4725665 A US4725665 A US 4725665A US 88835186 A US88835186 A US 88835186A US 4725665 A US4725665 A US 4725665A
- Authority
- US
- United States
- Prior art keywords
- formaldehyde
- water
- naphthalenesulfonic acid
- additive
- cement
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- 150000003839 salts Chemical class 0.000 title claims abstract description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 120
- 239000011230 binding agent Substances 0.000 claims abstract description 32
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000000463 material Substances 0.000 claims abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 43
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 38
- 239000011347 resin Substances 0.000 claims description 24
- 229920005989 resin Polymers 0.000 claims description 24
- 238000009833 condensation Methods 0.000 claims description 14
- 230000005494 condensation Effects 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 11
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 8
- 239000004014 plasticizer Substances 0.000 claims description 7
- 238000006277 sulfonation reaction Methods 0.000 claims description 4
- 238000010533 azeotropic distillation Methods 0.000 claims description 3
- 239000000654 additive Substances 0.000 abstract description 50
- 230000000996 additive effect Effects 0.000 abstract description 40
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004568 cement Substances 0.000 description 31
- 239000000203 mixture Substances 0.000 description 24
- 239000004567 concrete Substances 0.000 description 23
- 239000002245 particle Substances 0.000 description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 239000007787 solid Substances 0.000 description 9
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 8
- 229910052925 anhydrite Inorganic materials 0.000 description 7
- 239000004576 sand Substances 0.000 description 7
- 239000004566 building material Substances 0.000 description 6
- 239000011083 cement mortar Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000011148 porous material Substances 0.000 description 6
- 239000011398 Portland cement Substances 0.000 description 5
- 239000008032 concrete plasticizer Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- -1 for example Substances 0.000 description 4
- 239000004570 mortar (masonry) Substances 0.000 description 4
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000004572 hydraulic lime Substances 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- 229910003556 H2 SO4 Inorganic materials 0.000 description 1
- 240000006909 Tilia x europaea Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010883 coal ash Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011404 masonry cement Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000004573 non-hydraulic lime Substances 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229910021487 silica fume Inorganic materials 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/16—Sulfur-containing compounds
- C04B24/20—Sulfonated aromatic compounds
- C04B24/22—Condensation or polymerisation products thereof
- C04B24/226—Sulfonated naphtalene-formaldehyde condensation products
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G16/00—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
- C08G16/02—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
- C08G16/0212—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds
- C08G16/0218—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen
- C08G16/0237—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G16/00—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
- C08G16/02—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
- C08G16/04—Chemically modified polycondensates
Definitions
- the present invention relates to the use of additives based on naphthalenesulfonic acid/formaldehyde condensates for improving the properties, in particular the flowability, of inorganic binders, such as, for example, cement, anhydrite or gypsum, and the building material produced using this.
- inorganic binders such as, for example, cement, anhydrite or gypsum
- U.S. Pat. No. 2,141,569 has disclosed that the flowability of building materials based on cement can be increased by agents which have a dispersing action on the cement. If, on the other hand, the improved flowability made possible by the additive is dispensed with, an improvement in the strengths of the building materials produced with these additives over those without plasticizing additives is achieved, at constant flowability, by adding a relatively small amount of water to the cement mixture.
- concrete plasticizers of this type are obtained by condensation of aromatic sulfonic acids, such as, for example, naphthalenesulfonic acid, with formaldehyde at 95°-100° C.
- German Auslegeschrift 1,238,831 and British patent No. 1,286,798 describe naphthalenesulfonic acid/formaldehyde condensates in the form of concrete plasticizers having a molar formaldehyde/naphthalene ratio of 1:1, which are characterized by at least a 70% content of condensates having at least 5 naphthalene nuclei, and British patent No. 1,286,798 furthermore describes the addition of a gluconate.
- 1983-96618 likewise describes a concrete plasticizer which is based on naphthalene/formaldehyde and is obtained by condensation at 100°-140° C. in a nitrogen atmosphere under pressures up to 30 bar.
- the molar ratio of formaldehyde to naphthalene is formally claimed as 0.8-1.2, in the specific examples a ratio of 1.0 is used.
- the good properties are supposed to be attributable to the presence of inert gas in the pressure reactor.
- Japanese preliminary published application No. 1983-61115 describes a molar formaldehyde/naphthalene ratio of 0.7-1.1, preferably 0.9-1.05, and points out that a molar ratio above 1.1 gives too vigorous a reaction and products possessing poor properties.
- Naphthalenesulfonic acid/formaldehyde condensates which have a higher molar formaldehyde/naphthalene ratio of up to 3 but are added to the cement not to increase the flowability but, on the contrary, to reduce the water loss are described in U.S. Pat. No. 3,277,162.
- These so-called “water loss additives” are added to cements which are used for lining bore holes, for example in oil production. The action of the "water loss additives” is based on the fact that they are supposed to prevent loss of water from the cement mixture to the surrounding porous rock before the cement sets.
- naphthalenesulfonic acid resins which are used as concrete plasticizers should have a ratio of formaldehyde to naphthalenesulfonic acid of not more than 1:1; higher formaldehyde values in relation to the naphthalenesulfonic acid have an adverse effect on the plasticizing action.
- these known concrete plasticizers are not sufficiently active to permit them to be used in an optimum manner since they greatly increase the content of air pores in the fresh concrete at the same time and consequently decrease the strength of the ready-prepared concrete.
- naphthalenesulfonic acid/formaldehyde condensates having a higher formaldehyde/naphthalenesulfonic acid ratio than 1:1 give substantially improved flowability coupled with clearly reduced air pore formation, although such resins were expected to have a reduced action.
- the present invention accordingly relates to the use of salts of water-soluble naphthalenesulfonic acid/formaldehyde condensates, which have a molar ratio of formaldehyde to naphthalenesulfonic acid of 1.2:1 to 3:1 and are condensed to a degree of condensation which corresponds to an intrinsic viscosity of 0.01 to 0.15 dl/g, as additives for inorganic binders for increasing the flowability and, if required, the strength of the structural components produced from them.
- the intrinsic viscosity or the Staudinger index is defined in Kunststoff Handbuch, volume 1, page 736, published by Vieweg and Braun, Carl Hanser Verlag 1975, and is used for characterizing the molecular weight of the polycondensate. The determination was carried out according to DIN 51,562 in an Ubbelohde capillary viscometer in 1 N sodium nitrate solution at 30° C.
- the essential advantage of the invention is, in particular, that the flowability of the inorganic binders is increased without air pores additionally being introduced and the strength consequently reduced. This allows, on the one hand, binder mixtures to be transported without problems, in particular through pipelines, and on the other hand makes it possible completely to fill even poorly accessible and narrow sites and to cast relatively large flat surfaces so that they are self-leveling.
- Another advantage of the invention is that, when the additive according to the invention is used, the flowability of the mixture required for processing is achieved with the addition of only a small amount of water, with the result that the hardened building material possesses greater strength.
- naphthalenesulfonic acid/formaldehyde resins according to the invention arises from the fact that the early strengths of binders to which such resins are added are substantially higher than those of comparable binders containing conventional plasticizers.
- Inorganic binders are understood as being all substances used in the building industry, such as, for example, cements, plaster binders and masonry cements, hydraulic limes, non-hydraulic limes, building plasters, anhydrite binders, magnesite binders and mixed binders (mixture of hydraulic binder with pozzolanic materials, such as, for example, pulverized fuel ash or microporous silica), which are prepared with water and with or without additives, such as, for example, sand of different particle sizes, and with or without further additives, and, after hardening, give a stable structural component or a stable bond between prefabricated structural components.
- naphthalenesulfonic acid/formaldehyde resins having a molar formaldehyde/naphthalenesulfonic acid ratio of 1.3:1 to 3.0:1 are preferably employed since these give optimum results with regard to plasticizing and strength.
- naphthalenesulfonic acid/formaldehyde resins are those which are condensed up to a degree of condensation which corresponds to an intrinsic viscosity of 0.02 to 0.10 dl/g.
- the naphthalenesulfonic acid/formaldehyde resins according to the invention are preferably added to the binder mixture in an amount corresponding to 0.01 to 5% by weight, based on the binder content, of the solid resin.
- the addition of 0.2 to 1.5% by weight is particularly preferred since in this range an excellent plasticizing effect is achieved without having to use excessively large amounts of the resin.
- the naphthalene/formaldehyde resin can be added to the binder mixture both in solid form and in solution.
- naphthalenesulfonic acid/formaldehyde resins are advantageously used as plasticizers for inorganic binders, which are prepared by sulfonating naphthalene with concentrated sulfuric acid in a first reaction stage. The water formed during this procedure is removed simultaneously from the sulfonation mixture by azeotropic distillation with gasolene. Approximately molar amounts of sulfuric acid are therefore sufficient. A molar ratio of sulfuric acid to naphthalene of 0.9 to 1.1 is particularly preferred.
- the naphthalenesulfonic acid formed is then condensed with excess formaldehyde, and the procedure may be carried out either under atmospheric pressure or under superatmospheric pressure, pressures of 2.5 to 11 bar being preferred.
- the reaction temperature is preferably 110° to 160° C. It is not necessary to establish an inert gas atmosphere in the pressure zone. After the condensation, a pH value between 7.5 and 11 is established, for example the alkali metal, alkaline earth metal or ammonium salts being formed.
- the resin solution obtained is either employed as such or, if required, evaporated to dryness in a spray dryer, the resin being obtained in the form of a dry powder having a maximum water content of 10%.
- the kettle containing the cooled sulfonic acid was closed tightly, and 233.5 g of 36% strength formalin were then introduced in the course of one hour at 120° C. and under a pressure of 1-3 bar.
- the total amount of formaldehyde to naphthalene corresponded to a molar ratio of 1.22:1.
- the mixture was heated to 140° C., a pressure of 4.5 bar being established, and was stirred until the degree of condensation corresponded to an intrinsic viscosity of 0.04 dl/g in 1 N NaNO 3 at 30° C.
- the pressure was then let down, and the mixture was diluted with 360 g of water and cooled to 80° C.
- the acidic resin was brought to pH 8.0 with about 200 g of 50% strength NaOH and discharged into containers at room temperature.
- the concentration of naphthalene/formaledhyde resin in the solution was 40%.
- Resins having a different formaldehyde/naphthalenesulfonic acid ratio can be prepared in an analogous manner.
- the ratios are stated in the table below.
- the additive according to the invention was prepared in each case analogously to Example 1, except that different amounts of formalin were employed, as shown in table 1, resulting in the different molar ratios of formaldehyde to naphthalene in the finished resin, as shown in table 1.
- the resin content of the aqueous solutions obtained was 40% by weight.
- Example 5 The preparation and testing of the concrete mixtures were likewise carried out analogously to Example 1, the resin being added in solid form, after spray-drying in Example 5.
- the additive according to the invention was prepared in each case analogously to Example 1, except with a molar ratio of formaldehyde to naphthalene of 1.50, the process conditions stated in table 1 being maintained.
- the preparation and testing of the concrete mixture were carried out analogously to Example 1, except that, instead of PZ 275, a PZ 375 from Gmundner Zementtechnike H. Hatschek was employed in an amount of 420 kg/m 3 of fresh concrete, the amount of additive was varied from 0.02 to 10% by weight, based on the cement content, and different water/cement ratios (W/C ratio) were used.
- the results of the concrete test are reproduced in table 3.
- the slump prior to the addition of the additive was 44 cm for a water/cement ratio of 0.475.
- the said concrete mixture having a cement content of 300 kg/m 3 of solid concrete and being prepared analogously to Example 1, except with the addition of 0.8% of the plasticizer and with a water/cement ratio of 0.436 (130.71 of water/m 3 of concrete).
- a comparative sample without an additive was prepared analogously, an increased cement ratio of 357 kg of cement/m 3 of solid concrete being established in the comparative sample in order to achieve the same final strength. To achieve the same water/cement ratio, 196.4 1 of water/m 3 of solid concrete were added.
- the slump of an analogous cement mortar without an additive was 13 cm.
- An anhydrite mixture was prepared analogously, but without the addition of the additive, and with a water/anhydrite ratio of 0.601 in order to achieve an analogous flowability.
- the slump in cm as a measure of the flowability and the flexural tensile strength and compressive strength (4 ⁇ 4 ⁇ 16 cm prisms) were determined according to DIN 1164, sheets 5 and 7.
- a cement mortar to which 5.4 g of the additive according to the invention (1.22% based on the binder) and which was very readily homogenizable was prepared analogously.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Structural Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Abstract
Description
TABLE 1
______________________________________
Preparation of the additive
Formaldehyde/ Water (g)
naphthalene 36% strength
before after
Example
(mole/mole) formalin (g)
the condensation
______________________________________
1 1.22 233.5 292 360
2 1.30 248.8 280 364
3 1.50 287 273 380
4 2.00 383 239 405
5 2.50 477.5 205 411
6 3.00 574 170 450
7-16 1.50 287 273 380
17 1.22 233.5 292 364
18-20 1.50 287 273 380
______________________________________
TABLE 2
______________________________________
Properties of the concrete
300 kg of PZ 275/m.sup.3, water/cement ratio: 0.545
0.28% of additive
Formaldehyde/ Compressive Air
naphthalene Slump strength (MPa)
pores
Example
(mole/mole) (cm) 18 h 28 days
(%)
______________________________________
Blank -- 33.5 9.7 37.1 1.1
test
1 1.22 60 10.8 37.5 1.1
2 1.30 59 10.5 38.1 1.0
3 1.50 61 10.2 38.0 0.9
4 2.00 62 10.4 39.9 0.9
5 2.50 59 10.5 40.0 1.0
6 3.00 59 10.3 40.2 1.0
______________________________________
TABLE 3
______________________________________
Properties of the concrete 420 kg of PZ 375/m.sup.3
Compressive
strength Air
Additive
Slump (MPa) pores
Example
W/C ratio (%) (cm) 18 h 28 days
(%)
______________________________________
7 0.475 0.02 49 13.5 45.6 less
than
0.9
8 0.475 0.05 54 17.5 45.9 less
than
0.9
9 0.34 5.0 60 18.2 55.1 2.0
10 0.34 10.0 58 7.0 50.8 2.4
______________________________________
______________________________________
Compressive strength
Water/cement Slump (MPa)
ratio (cm) 18 h 28 days
______________________________________
No additive
0.533 42.0 9.15 38.1
0.8% of 0.436 42.5 14.40 44.5
additive
______________________________________
______________________________________
kg of cement/ Water/ Compressive
m.sup.3 of cement Slump strength (MPa)
concrete ratio (cm) 18 h 28 days
______________________________________
No additive
357 0.55 50 9.25 40
0.52% of
298 0.55 50 11.65 40
additive
______________________________________
TABLE 4
______________________________________
Intrinsic viscosity
Slump
Example (dl/g) (cm)
______________________________________
13 0.017 16
14 0.034 27.5
15 0.104 15
16 0.15 14
______________________________________
______________________________________
Flexural
Compressive tensile
strength strength
Water/ Slump (MPa) (MPa)
anhydrite (cm) 28 days 28 days
______________________________________
No additive
0.601 20 8.97 3.22
0.38% of
0.377 20 37.50 8.26
additive
______________________________________
______________________________________
Flexural
tensile Compressive
Slump strength strength
W/B ratio
(cm) 18 h (mPa)
______________________________________
No additive
0.9 13.1 1.1 2.9
1.22% of 0.9 21.2 1.1 2.1
additive
1.22% of 0.478 13.1 2.47 8.55
additive
______________________________________
______________________________________
Flexural
tensile Compressive
strength strength
Slump 7 days 7 days
W/B ratio
(cm) (MPa) (MPa)
______________________________________
No additive
0.45 13.5 4.8 25.7
0.4% of 0.45 18.2 4.3 23.3
additive
______________________________________
______________________________________
Flexural
tensile Compressive
strength strength
Slump 7 days 7 days
W/B ratio
(cm) (MPa) (MPa)
______________________________________
No additive
0.5 11.5 0.91 4.9
1.2% of 0.5 19.5 1.6 6.4
additive
______________________________________
Claims (8)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19853530258 DE3530258A1 (en) | 1985-08-23 | 1985-08-23 | USE OF SALTS OF WATER-SOLUBLE NAPHTALINE SULPHONIC ACID FORMALDEHYDE CONDENSATES AS ADDITIVES FOR INORGANIC BINDERS AND BUILDING MATERIAL |
| DE3530258 | 1985-08-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4725665A true US4725665A (en) | 1988-02-16 |
Family
ID=6279251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/888,351 Expired - Fee Related US4725665A (en) | 1985-08-23 | 1986-07-23 | Use of salts of water-soluble |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4725665A (en) |
| EP (1) | EP0214412B1 (en) |
| JP (1) | JPH07106933B2 (en) |
| AT (1) | ATE62007T1 (en) |
| DE (2) | DE3530258A1 (en) |
| DK (1) | DK169431B1 (en) |
| NO (1) | NO170212C (en) |
Cited By (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4935060A (en) * | 1987-11-16 | 1990-06-19 | Elkem A/S | Hydraulic cement slurry |
| DE4007459A1 (en) * | 1990-03-09 | 1991-09-19 | Chemie Linz Deutschland | Naphthalene-sulphonic-formaldehyde condensates with low free aldehyde - obtd. by immediately adjusting the condensation prod. up to specific pH at 80 deg. C., etc. |
| US5101007A (en) * | 1990-02-19 | 1992-03-31 | Chemie Linz Gesellschaft M.B.H. | Process for the preparation of naphthalenesulfonic acid/formaldehyde condensates having a low free formaldehyde content |
| US5206336A (en) * | 1990-02-19 | 1993-04-27 | Chemie Linz Gesellschaft M.B.H. | Process for the preparation of naphthalenesulfonic acid/formaldehyde condensates having a low free formaldehyde content |
| US5284741A (en) * | 1989-12-11 | 1994-02-08 | Konica Corporation | Antistatic layer |
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Cited By (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4935060A (en) * | 1987-11-16 | 1990-06-19 | Elkem A/S | Hydraulic cement slurry |
| US5284741A (en) * | 1989-12-11 | 1994-02-08 | Konica Corporation | Antistatic layer |
| US5101007A (en) * | 1990-02-19 | 1992-03-31 | Chemie Linz Gesellschaft M.B.H. | Process for the preparation of naphthalenesulfonic acid/formaldehyde condensates having a low free formaldehyde content |
| US5206336A (en) * | 1990-02-19 | 1993-04-27 | Chemie Linz Gesellschaft M.B.H. | Process for the preparation of naphthalenesulfonic acid/formaldehyde condensates having a low free formaldehyde content |
| DE4007459A1 (en) * | 1990-03-09 | 1991-09-19 | Chemie Linz Deutschland | Naphthalene-sulphonic-formaldehyde condensates with low free aldehyde - obtd. by immediately adjusting the condensation prod. up to specific pH at 80 deg. C., etc. |
| US5369198A (en) * | 1993-02-01 | 1994-11-29 | Chemie Linz Gesellschaft M.B.H | Copolymers based on maleic acid derivatives and vinyl monomers, their production and application |
| FR2740445A1 (en) * | 1995-10-27 | 1997-04-30 | Francais Ciments | ADDITIVE TO MONITOR THE SEDIMENTATION OF CONGLOMERATES |
| EP0770585A1 (en) * | 1995-10-27 | 1997-05-02 | Ciments Francais | Additive for controlling the sedimentation of conglomerates |
| EP1074528A1 (en) * | 1999-08-04 | 2001-02-07 | Clariant GmbH | Use of dispersion powders, comprising water soluble salts of sulphonated formaldehyde condensation products, in hydraulically setting masses |
| US20040092676A1 (en) * | 2002-08-07 | 2004-05-13 | Geo Specialty Chemicals, Inc. | Dispersant and foaming agent combination |
| US20040091751A1 (en) * | 2002-08-07 | 2004-05-13 | Geo Specialty Chemicals, Inc. | Method of making wallboard |
| US6774146B2 (en) | 2002-08-07 | 2004-08-10 | Geo Specialty Chemicals, Inc. | Dispersant and foaming agent combination |
| US6929875B2 (en) | 2002-08-07 | 2005-08-16 | Geo Specialty Chemicals, Inc. | Method of making wallboard |
| US20050224007A1 (en) * | 2002-08-07 | 2005-10-13 | Geo Specialty Chemicals, Inc. | Plaster composition and method of making same |
| US7033432B2 (en) | 2002-08-07 | 2006-04-25 | Geo Speciality Chemicals, Inc. | Plaster composition and method of making same |
| US20060183879A1 (en) * | 2005-01-31 | 2006-08-17 | Kao Corporation | Process for producing a naphthalenesulfonate formaldehyde condensate |
| US20090209682A1 (en) * | 2005-07-18 | 2009-08-20 | Bernhard Sturm | Use of an organic additve for producing porous concrete |
| WO2011026723A1 (en) | 2009-09-02 | 2011-03-10 | Construction Research & Technology Gmbh | Sulphonic acid and aromatic groups containing hardening accelerator compositions |
| US20110054053A1 (en) * | 2009-09-02 | 2011-03-03 | Lee Chris C | Additives in gypsum panels and adjusting their proportions |
| US20110054081A1 (en) * | 2009-09-02 | 2011-03-03 | Frank Dierschke | Formulation and its use |
| US8597426B2 (en) | 2009-09-02 | 2013-12-03 | United States Gypsum Company | Additives in gypsum panels and adjusting their proportions |
| US8801852B2 (en) | 2009-09-02 | 2014-08-12 | United States Gypsum Company | Additives in gypsum slurries and adjusting their proportions |
| US9353007B2 (en) | 2009-11-11 | 2016-05-31 | Basf Construction Polymers Gmbh | Dry mortar mixture |
| US8940832B2 (en) | 2010-02-26 | 2015-01-27 | Clariant Finance (Bvi) Limited | Polymers and use thereof as dispersants having a foam-inhibiting effect |
| CN101880247A (en) * | 2010-05-31 | 2010-11-10 | 杭州吉华江东化工有限公司 | Method for producing naphthalene sulfonic formaldehyde condensation compound |
| US8906986B2 (en) | 2010-12-09 | 2014-12-09 | Basf Construction Solutions Gmbh | Additive for building product mixtures containing flow agents |
| US9018337B2 (en) | 2011-01-26 | 2015-04-28 | Construction Research & Technology Gmbh | Process for producing polycondensation product |
| US10273188B2 (en) | 2011-09-30 | 2019-04-30 | Basf Construction Solutions Gmbh | Powder composition for rapid suspension |
| US10392306B2 (en) | 2012-04-11 | 2019-08-27 | Construction Research & Technology Gmbh | Polycondensation product based on aromatic compounds, method for the preparation and use thereof |
| US9388077B2 (en) | 2012-08-13 | 2016-07-12 | Construction Research & Technology Gmbh | Hardening accelerator composition |
| US9650298B2 (en) | 2012-08-13 | 2017-05-16 | Construction Research & Technology Gmbh | Hardening accelerator composition for cementitious compositions |
| US9522996B2 (en) | 2013-03-26 | 2016-12-20 | Basf Se | Composition comprising a copolymer |
| US10266700B2 (en) | 2013-03-26 | 2019-04-23 | Basf Se | Rapidly suspendable pulverulent composition |
| US9586864B2 (en) | 2013-03-26 | 2017-03-07 | Basf Se | Rapidly suspendable pulverulent composition |
| US10174144B2 (en) | 2013-09-27 | 2019-01-08 | Construction Research & Technology, Gmbh | Cationic copolymers |
| US9803053B2 (en) | 2013-12-20 | 2017-10-31 | Construction Research & Technology, Gmbh | Additive for rheology improvement of inorganic binders |
| US10005695B2 (en) | 2014-06-06 | 2018-06-26 | Basf Se | Composition based on calcium silicate hydrate |
| US10065891B2 (en) | 2014-11-10 | 2018-09-04 | Basf Se | Polymer having polyether side chains |
| US10865144B2 (en) | 2015-03-13 | 2020-12-15 | Basf Se | Method for producing a dispersant |
| US11485683B2 (en) | 2015-12-17 | 2022-11-01 | Construction Research & Technology Gmbh | Polycondensate based water-reducer |
| WO2020089271A1 (en) | 2018-10-31 | 2020-05-07 | Basf Se | Enhanced dewatering of mining tailings employing chemical pre-treatment |
Also Published As
| Publication number | Publication date |
|---|---|
| DK169431B1 (en) | 1994-10-31 |
| JPS6246946A (en) | 1987-02-28 |
| EP0214412B1 (en) | 1991-03-27 |
| DE3530258A1 (en) | 1987-02-26 |
| NO170212C (en) | 1992-09-23 |
| NO863068L (en) | 1987-02-24 |
| DE3678364D1 (en) | 1991-05-02 |
| NO170212B (en) | 1992-06-15 |
| NO863068D0 (en) | 1986-07-29 |
| DK400686D0 (en) | 1986-08-22 |
| ATE62007T1 (en) | 1991-04-15 |
| EP0214412A1 (en) | 1987-03-18 |
| JPH07106933B2 (en) | 1995-11-15 |
| DK400686A (en) | 1987-02-24 |
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